Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:22052500-22052760 | Common:3; Rare:90 | ||||
chr1:23019304-23019545 | Rare:81 | ||||
chr1:23019900-23019936 | Rare:5 | ||||
chr1:23344214-23344592 | Common:2; Rare:132 | ||||
chr1:23368188-23368523 | Common:1; Rare:96 | ||||
chr1:23368776-23369010 | Common:2; Rare:75 | ||||
chr1:23559434-23559643 | Common:1; Rare:92 | ||||
chr1:23743210-23743510 | Rare:109 | ||||
chr1:23778236-23778504 | Common:9; Rare:136 | ||||
chr1:23790995-23791247 | Rare:75 | ||||
chr1:23800723-23800959 | Common:1; Rare:84 | ||||
chr1:23825405-23825556 | Common:2; Rare:47; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959608-23959862 | Common:2; Rare:68 | ||||
chr1:23960023-23960192 | Common:1; Rare:51 | ||||
chr1:23980174-23980573 | Common:1; Rare:114 |